Abstract
We present a new concept for tri-analyte DNA detection based on the idea of a Y-shaped capture probe which, after tri-target and fluorescently labeled reporter probe binding, becomes colour-coded to generate images in an RGB colour scheme. Hence, the RGB value of the resulting secondary pseudo-colour presented by the hybridized Y-DNA can be related to the ratio of the primary pseudo-colours present in its make-up, and thus to the ratio of the three target concentrations. As a proof of concept we detect sequences from the genes of the pathogenic bacterial strains Escherichia coli O157:H7, Vibrio cholera and Salmonella enteric in a semi-quantitative manner across the range 20-167. nM. The assay was relatively quick, with a time from hybridization to completed data interpretation of approximately 4. h.
| Original language | English |
|---|---|
| Pages (from-to) | 2183-2187 |
| Number of pages | 5 |
| Journal | Biosensors and Bioelectronics |
| Volume | 26 |
| Issue number | 5 |
| DOIs | |
| Publication status | Published - 15 Jan 2011 |
| Externally published | Yes |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
-
SDG 3 Good Health and Well-being
Keywords
- Colocalization
- DNA detection
- Fluorescence
- Multicolour
- Multiplex
Fingerprint
Dive into the research topics of 'RGB colour coding of Y-shaped DNA for simultaneous tri-analyte solid phase hybridization detection'. Together they form a unique fingerprint.Cite this
- APA
- Author
- BIBTEX
- Harvard
- Standard
- RIS
- Vancouver